Baylin S B, Margolis S
Biochim Biophys Acta. 1975 Aug 26;397(2):294-306. doi: 10.1016/0005-2744(75)90119-9.
The present study describes the use of affinity chromatography to achieve a high degree of purification of histaminase (diamine oxidase, EC 1.4.3.6) from plasma of women in the third trimester of pregnancy. The procedure is based upon the binding of histaminase to cadaverine, a diamine substrate for the enzyme, which is coupled to Sepharose. Contaminant proteins were removed by high concentrations of NaCl (up to 1.0M), and the histaminase was then eluted from the column with a buffer containing 300--400 units/ml of sodium heparin. The purification technique has the following characteristics: (1) in optimal experiments, 3000-fold purification of enzyme was obtained; (2) the yield of enzyme was as great as 25%; (3) the binding of histaminase to the amine groups of the cadaverine appears to represent a true "affinity" phenomenon since enzyme bound to DEAE-cellulose under neutral pH conditions was eluted at much lower concentrations of NaCl (less than 0.4 M). The enzyme purified by the present procedure has the following properties: (1) disc gel polyacrylamide electrophoresis showed two protein bands for 1000--3000-fold pure histaminase; the major band may represent a contaminant protein, while the minor band corresponded to the position of histaminase activity; (2) a 90 000 molecular weight subunit for the plasma histaminase was identified on calibrated sodium dodecyl sulfate gels; this value agrees well with previous estimations for the subunit size of human placental histaminase; (3) the purified enzyme behaved as classical histaminase (diamine oxidase) in that it was totally inhibited by low concentrations of aminoguanidine, but was less inhibited by semicarbazide and by inhibitors of monoamine oxidase, and the enzyme was active against histamine and putrescine, but not against the monoamines benzylamine and tryptamine. Also, the enzyme was strongly inhibited by NaCl.
本研究描述了使用亲和色谱法从妊娠晚期妇女血浆中高度纯化组胺酶(二胺氧化酶,EC 1.4.3.6)的方法。该方法基于组胺酶与尸胺(该酶的二胺底物)的结合,尸胺与琼脂糖偶联。通过高浓度的氯化钠(高达1.0M)去除污染蛋白,然后用含有300 - 400单位/毫升肝素钠的缓冲液从柱上洗脱组胺酶。该纯化技术具有以下特点:(1)在最佳实验中,酶得到了3000倍的纯化;(2)酶的产量高达25%;(3)组胺酶与尸胺胺基的结合似乎代表了一种真正的“亲和”现象,因为在中性pH条件下与DEAE - 纤维素结合的酶在低得多的氯化钠浓度(小于0.4M)下被洗脱。通过本方法纯化的酶具有以下特性:(1)圆盘凝胶聚丙烯酰胺电泳显示,1000 - 3000倍纯的组胺酶有两条蛋白带;主要条带可能代表一种污染蛋白,而次要条带对应于组胺酶活性的位置;(2)在经校准的十二烷基硫酸钠凝胶上鉴定出血浆组胺酶的分子量为90000的亚基;该值与先前对人胎盘组胺酶亚基大小的估计非常吻合;(3)纯化后的酶表现为经典的组胺酶(二胺氧化酶),即它被低浓度的氨基胍完全抑制,但被氨基脲和单胺氧化酶抑制剂抑制的程度较小,并且该酶对组胺和腐胺有活性,但对单胺苄胺和色胺无活性。此外,该酶被氯化钠强烈抑制。